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Submitted SNP(ss) Details: ss294688725           
Submitter
HandlePJP
Submitter SNP IDDIP_126429_chr11_10541070
RefSNP(rs#)rs71034774
Submitted Batch IDNSMB2011_INDEL
Submitted DateJan 21, 2011
Publication Cited[1] Impact of chromatin structure on sequence variability in the human genome
First entry to dbSNPJan 21 2011 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodTRACESALIGNMENT
Ascertainment SamplesizeN.D.
PopulationN.D.
Allele
Observed Allele-/T
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassDIV
CpG CodeN.D.
Validation
Validation StatusNot Validated
HWE Goodness of Fitnot applicable
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss294688725|allelePos=52|len=103|taxid=9606|alleles='-/T'|mol=Genomic
 CAGTAATGAG ACGTTAGACA AATGTGTTTA CATCCTTTGA ACTCGGTTTC T
 N
 TTTTTTTTTT TTTTTTTTTT TTTTGAGACG GAGTCTCACT CTGTCGCCCA G

  Submitted Frequency for ss294688725 back to top
There is no frequency submission for ss294688725.


  dbSNP summary of Genotypes for ss294688725 back to top
No sufficient data to compute Hardy-weinberg probability for ss294688725.


  Submitted individual genotype for ss294688725 back to top
There is no individual genotype data for ss294688725.

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